Variant #0000480271 (NC_000019.9:g.13002736del, NM_000159.3:c.219del (GCDH))
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
ACMG |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13002736del |
DNA change (hg38) |
g.12891922del |
Published as |
- |
ISCN |
- |
DB-ID |
GCDH_000066 See all 10 reported entries |
Variant remarks |
ACMG/ACGS: PS4_Moderate, PM3_Strong, PP4, PVS1, PM2_Supporting (December 2023) |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Isabelle Rinke |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2019-05-22 09:22:27 +02:00 (CEST) |
Date last edited |
2024-11-11 14:57:23 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|